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The Journal of Neuroscience, August 27, 2003, 23(21):7783-7788
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Transplanted Olfactory Ensheathing Cells Promote Regeneration of Cut Adult Rat Optic Nerve Axons
Ying Li,1
Yves Sauvé,2
Daqing Li,1
Raymond D. Lund,2 and
Geoffrey Raisman1
1Division of Neurobiology, Norman and Sadie Lee
Research Centre, Medical Research Council National Institute for Medical
Research, London NW7 1AA, United Kingdom, and 2 Moran
Eye Center, University of Utah Health Sciences Center, Salt Lake City, Utah
84132
Transplantation of olfactory ensheathing cells into spinal cord lesions
promotes regeneration of cut axons into terminal fields and functional
recovery. This repair involves the formation of a peripheral
nerve-like bridge in which perineurial-like fibroblasts are organized into a
longitudinal stack of parallel tubular channels, some of which contain
regenerating axons enwrapped by Schwann-like olfactory ensheathing cells. The
present study examines whether cut retinal ganglion cell axons will also
respond to these cells, and if so, whether they form the same type of
arrangement. In adult rats, the optic nerve was completely severed behind the
optic disc, and a matrix containing cultured olfactory ensheathing cells was
inserted between the proximal and distal stumps. After 6 months, the
transplanted cells had migrated for up to 10 mm into the distal stump.
Anterograde labeling with cholera toxin B showed that cut retinal ganglion
cell axons had regenerated through the transplants, entered the distal stump,
and elongated for 10 mm together with the transplanted cells. Electron
microscopy showed that a peripheral nerve-like tissue had been formed, similar
to that seen in the spinal cord transplants. However, in contrast to the
spinal cord, the axons did not reach the terminal fields, but terminated in
large vesicle-filled expansions beyond which the distal optic nerve stump was
reduced to a densely interwoven mass of astrocytic processes.
Key words: regeneration; CNS; adult; vision; eye; OECs; transplantation
Received June 2, 2003;
revised July 7, 2003;
accepted July 8, 2003.
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